Canonical Allele Identifier: CA59780683
Gene: SCN9A HGNC NCBI
SCN1A-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs145255931
MyVariant Identifiers: chr2:g.167052555_167052556insTTAAAAAAGTT (hg19) chr2:g.166196045_166196046insTTAAAAAAGTT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.166196048_166196058dup , CM000664.2:g.166196048_166196058dup GRCh38
NC_000002.11:g.167052558_167052568dup , CM000664.1:g.167052558_167052568dup GRCh37
NC_000002.10:g.166760804_166760814dup NCBI36
NG_012798.1:g.184932_184942dup , LRG_369:g.184932_184942dup

Transcript Alleles

HGVS Amino-acid change
ENST00000303354.11:c.*2616_*2626dup (SCN9A) ENSP00000304748.7:n.*2616_*2626dup
ENST00000642356.2:c.*2616_*2626dup (SCN9A) MANE Select ENSP00000495601.1:n.*2616_*2626dup
ENST00000303354.10:c.*2616_*2626dup (SCN9A) ENSP00000304748.7:n.*2616_*2626dup
ENST00000409672.5:c.*2616_*2626dup (SCN9A) ENSP00000386306.1:n.*2616_*2626dup
NM_002977.3:c.*2616_*2626dup , LRG_369t1:c.*2616_*2626dup (SCN9A) NP_002968.1:n.*2616_*2626dup
NR_110260.1:n.432-3591_432-3581dup (SCN1A-AS1)
NM_001365536.1:c.*2616_*2626dup (SCN9A) MANE Select NP_001352465.1:n.*2616_*2626dup
Search 100 bp 5'
Search 100 bp 3'